Global Variome shared LOVD

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Phenotype #0000129776 Individual ID 00164737 Associated disease ? Diagnosis/Initial - Diagnosis/Definite COXPD-2 Phenotype details see paper; ..., agenesis of corpus callosum, dysmorphism, fatal neonatal lactic acidosis Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2018-06-07 08:28:11 +02:00 (CEST) Date last edited N/A

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